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Anti-VEGFR2 F(ab′)2 drug conjugate promotes renal accumulation and glomerular repair in diabetic nephropathy

Author

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  • Di Liu

    (College of Pharmaceutical Sciences, Zhejiang University)

  • Yanling Song

    (College of Pharmaceutical Sciences, Zhejiang University)

  • Hui Chen

    (College of Pharmaceutical Sciences, Zhejiang University)

  • Yuchan You

    (College of Pharmaceutical Sciences, Zhejiang University)

  • Luwen Zhu

    (College of Pharmaceutical Sciences, Zhejiang University)

  • Jucong Zhang

    (College of Pharmaceutical Sciences, Zhejiang University)

  • Xinyi Xu

    (College of Pharmaceutical Sciences, Zhejiang University)

  • Jiahao Hu

    (College of Pharmaceutical Sciences, Zhejiang University)

  • Xiajie Huang

    (College of Pharmaceutical Sciences, Zhejiang University)

  • Xiaochuan Wu

    (College of Pharmaceutical Sciences, Zhejiang University)

  • Xiaoling Xu

    (Zhejiang Shuren University)

  • Saiping Jiang

    (The First Affiliated Hospital, College of Medicine, Zhejiang University)

  • Yongzhong Du

    (College of Pharmaceutical Sciences, Zhejiang University
    Jinhua Institute of Zhejiang University)

Abstract

Poor renal distribution of antibody-based drugs is the key factor contributing to low treatment efficiency for renal diseases and side effects. Here, we prepare F(ab′)2 fragmented vascular endothelial growth factor receptor 2 antibody (anti-VEGFR2 (F(ab′)2) to block VEGFR2 overactivation in diabetic nephropathy (DN). We find that the anti-VEGFR2 F(ab′)2 has a higher accumulation in DN male mice kidneys than the intact VEGFR2 antibody, and simultaneously preserves the binding ability to VEGFR2. Furthermore, we develop an antibody fragment drug conjugate, anti-VEGFR2 F(ab′)2-SS31, comprising the anti-VEGFR2 F(ab′)2 fragment linked to the mitochondria-targeted antioxidant peptide SS31. We find that introduction of SS31 potentiates the efficacy of anti-VEGFR2 F(ab′)2. These findings provide proof of concept for the premise that antibody fragment drug conjugate improves renal distribution and merits drug validation in renal disease therapy.

Suggested Citation

  • Di Liu & Yanling Song & Hui Chen & Yuchan You & Luwen Zhu & Jucong Zhang & Xinyi Xu & Jiahao Hu & Xiajie Huang & Xiaochuan Wu & Xiaoling Xu & Saiping Jiang & Yongzhong Du, 2023. "Anti-VEGFR2 F(ab′)2 drug conjugate promotes renal accumulation and glomerular repair in diabetic nephropathy," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-43847-2
    DOI: 10.1038/s41467-023-43847-2
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    References listed on IDEAS

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    1. Neil C. Henderson & Florian Rieder & Thomas A. Wynn, 2020. "Fibrosis: from mechanisms to medicines," Nature, Nature, vol. 587(7835), pages 555-566, November.
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